Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada.
Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada; Department of Biological Sciences, University of Calgary, Calgary, AB, Canada.
J Cyst Fibros. 2019 Nov;18(6):829-837. doi: 10.1016/j.jcf.2019.02.010. Epub 2019 Mar 8.
To improve clinical outcomes, cystic fibrosis (CF) patients with chronic Pseudomonas aeruginosa infections are prescribed inhaled anti-pseudomonal antibiotics. Although, a diverse microbial community exists within CF airways, little is known about how the CF microbiota influences patient outcomes. We hypothesized that organisms within the CF microbiota are affected by inhaled-antibiotics and baseline microbiome may be used to predict therapeutic response.
Adults with chronic P. aeruginosa infection from four clinics were observed during a single 28-day on/off inhaled-aztreonam cycle. Patients performed serial sputum collection, CF-respiratory infection symptom scores (CRISS), and spirometry. Patients achieving a decrease of ≥2 CRISS by day 28 were categorized as subjective responders (SR). The airway microbiome was defined by Illumina MiSeq analysis of the 16S rRNA gene.
Thirty-seven patients (median 37.4 years and FEV 44% predicted) were enrolled. No significant cohort-wide changes in the microbiome were observed between on/off AZLI cycles in either alpha- or beta-diversity metrics. However, at an individual level shifts were apparent. Twenty-one patients (57%) were SR and fourteen patients did not subjectively respond. While alpha-diversity metrics did not associate with response, patients who did not subjectively respond had a higher abundance of Staphylococcus and Streptococcus, and lower abundance of Haemophilus.
The CF microbiome is relatively resilient to AZLI perturbations. However, associated changes were observed at the individual patient level. The relative abundance of key "off-target" organisms associated with subjective improvements suggesting that the microbiome may be used as a tool to predict patient response - potentially improving outcomes.
为了改善临床结果,患有慢性铜绿假单胞菌感染的囊性纤维化 (CF) 患者被开处吸入型抗假单胞菌抗生素。尽管 CF 气道中存在多种微生物群落,但人们对 CF 微生物组如何影响患者结局知之甚少。我们假设 CF 微生物组中的生物受吸入型抗生素的影响,且基线微生物组可用于预测治疗反应。
来自四个诊所的慢性铜绿假单胞菌感染的成年患者在一个为期 28 天的吸入-氨曲南开/关周期中接受观察。患者进行连续的痰采集、CF 呼吸道感染症状评分(CRISS)和肺活量测定。在第 28 天达到 CRISS 下降≥2 的患者被归类为主观应答者(SR)。气道微生物组通过 Illumina MiSeq 分析 16S rRNA 基因来定义。
共纳入 37 名患者(中位年龄 37.4 岁,FEV 44%预计值)。在 AZLI 开/关周期中,无论是在 alpha 多样性还是 beta 多样性指标上,都没有观察到整个队列的微生物组发生显著变化。然而,在个体水平上则出现了明显的变化。21 名患者(57%)为 SR,14 名患者未出现主观应答。虽然 alpha 多样性指标与应答无关,但未出现主观应答的患者中葡萄球菌属和链球菌属的丰度较高,而嗜血杆菌属的丰度较低。
CF 微生物组对 AZLI 干扰具有相对弹性。然而,在个体患者水平上观察到了相关变化。与主观改善相关的关键“非靶标”生物的相对丰度表明,微生物组可能被用作预测患者应答的工具-从而有可能改善结局。